The metrics on this programme look excellent and it's a separate step; after assembly.
I am currently working on some de novo genome assembly with pacBio data. I used Canu for assembly but I didn't have access to quiver (or arrow) for data polishing. What can I do now? I can't find any tools for replace quiver, so I'm a little bit stuck...
Thanks !
3 answers
A new polisher called ntedit https://github.com/bcgsc/ntEdit is another alternative to RACON and wtdbg2 polishing.
It is an old thread, but as there are no answers on which polishers to use, I will add my experience.
I have tested wtdbg2 polishing module and Racon. Both provided good improvements over either a miniasm or wtdbg2 assemblies - I would imagine they would work fine for a Canu assembly as well. I also performed a Flye assembly, which has a built-in polishing step, and for my data, Flye resulted in the best assembly as per BUSCO evaluation.
Hei,Pacbio have there assembly pipeline ,if you use the canu ,just use the canu to assembly subreads fasta,needn't to polish the reads,canu can do it !
Alex
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